Canonical Allele Identifier: PA2825269225
Gene: NFASC HGNC NCBI
ClinVar RCV:
RCV003362413
ClinVar Variation:
2613546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005389.2:p.Pro7Leu
CA1349365
NM_001005389.2:c.20C>T